Thromb Haemost 2007; 98(06): 1316-1322
DOI: 10.1160/TH07-05-0323
Platelets and Blood Cells
Schattauer GmbH

Effect of clopidogrel treatment on stress-induced platelet activation and myocardial ischemia in aspirin-treated patients with stable coronary artery disease

Christina Perneby
1   Karolinska Institutet; Department of Medicine, Clinical Pharmacology Unit, Karolinska University Hospital, Stockholm, Sweden
,
Håkan N. Wallén
1   Karolinska Institutet; Department of Medicine, Clinical Pharmacology Unit, Karolinska University Hospital, Stockholm, Sweden
2   Department of Clinical Sciences, Danderyd Hospital, Stockholm, Sweden
,
Claes Hofman-Bang
2   Department of Clinical Sciences, Danderyd Hospital, Stockholm, Sweden
,
Per Tornvall
3   Cardiology Unit, Department of Molecular Medicine and Surgery, Karolinska University Hospital, Stockholm, Sweden
,
Torbjörn Ivert
4   Thoracic Surgery Unit, Karolinska University Hospital, Stockholm, Sweden
,
Nailin Li
1   Karolinska Institutet; Department of Medicine, Clinical Pharmacology Unit, Karolinska University Hospital, Stockholm, Sweden
,
Paul Hjemdahl
1   Karolinska Institutet; Department of Medicine, Clinical Pharmacology Unit, Karolinska University Hospital, Stockholm, Sweden
› Author Affiliations
Further Information

Publication History

Received 04 May 2007

Accepted after resubmission 06 September 2007

Publication Date:
30 November 2017 (online)

Summary

Stress may counteract responses to antiplatelet drug treatment. We investigated if adding clopidogrel to aspirin treatment could attenutate stress-induced platelet activation and myocardial ischemia in patients with coronary artery disease (CAD). Thirty-one male patients with documented CAD-treated with aspirin (75–160 mg daily) were randomized to co-treatment with clopidogrel (n=16) or placebo (n=15). A symptom-limited exercise test and 48-hour (h) Holter monitoring were performed before and after two weeks of double-blind treatment. Platelet function was assessed by flow cytometry and impedance aggregometry in whole blood. Exercise-induced and ambulatory ischemia was assessed from electrocardiographic (ECG) recordings. Clopidogrel treatment inhibited ADP-induced platelet P-selectin expression by 64% (22–87%), and attenuated the P-selectin response to thrombin (p<0.001), and platelet aggregation induced by low-dose collagen (p<0.01). Exercise (≈110W) increased heart rate similarly, and caused ≈1.8 mm STsegment depression both before and after treatment. Exercise caused platelet activation, i.e. increased circulating activated single platelets and platelet-platelet aggregates, enhanced the invitro responsiveness to ADP or thrombin stimulation, and increased platelet-leukocyte aggregation. Clopidogrel inhibited ADP-induced platelet activation to a similar relative degree at rest and during exercise, but did not attenuate the platelet activating effect of exercise. Addition of clopidogrel to aspirin treatment did not attenuate either ambulatory or exercise-induced ischemia. In conclusion, adding clopidogrel to aspirin treatment inhibited platelet activation by both ADP, thrombin and collagen in vitro,but did not influence the prothrombotic responses to exercise. Intensified antiplatelet treatment did not reduce ECG signs of either exercise-induced or ambulatory myocardial ischemia.

 
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